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WormBase Tree Display for Gene: WBGene00001494

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Name Class

WBGene00001494SMapS_parentSequenceH09G03
IdentityVersion1
NameCGC_namefrm-8Person_evidenceWBPerson204
Sequence_nameH09G03.2
Molecular_nameH09G03.2a
H09G03.2a.1
CE31024
H09G03.2b
CE31025
H09G03.2c
CE32455
H09G03.2b.1
H09G03.2c.1
Other_nameCELE_H09G03.2Accession_evidenceNDBBX284603
Public_namefrm-8
DB_infoDatabase (11)
SpeciesCaenorhabditis elegans
HistoryVersion_change107 Apr 2004 11:29:24WBPerson1971EventImportedInitial conversion from geneace
StatusLive
Gene_infoBiotypeSO:0001217
Gene_classfrm
Allele (521)
StrainWBStrain00032198
RNASeq_FPKM (74)
Ortholog (40)
Structured_descriptionConcise_descriptionfrm-8 encodes a protein containing a WW domain, a PDZ domain, and a FERM domain and has homology to the human predicted protein KIAA0316.Curator_confirmedWBPerson48
Date_last_updated17 Jun 2004 00:00:00
Automated_descriptionExpressed in PVDL and PVDR. Human ortholog(s) of this gene implicated in non-syndromic X-linked intellectual disability 104. Human FRMPD4 enables phosphatidylinositol-4,5-bisphosphate binding activity. Is predicted to encode a protein with the following domains: WW domain; Ras association (RalGDS/AF-6) domain; FERM central domain; FERM superfamily, second domain; FERM/acyl-CoA-binding protein superfamily; Ubiquitin-like domain superfamily; PDZ superfamily; Band 4.1 domain; and PDZ domain. Is an ortholog of human FRMPD1 (FERM and PDZ domain containing 1); FRMPD3 (FERM and PDZ domain containing 3); and FRMPD4 (FERM and PDZ domain containing 4).Paper_evidenceWBPaper00065943
Curator_confirmedWBPerson324
WBPerson37462
Inferred_automaticallyThis description was generated automatically by a script based on data from the WS291 version of WormBase
Date_last_updated29 Nov 2023 00:00:00
Disease_infoPotential_modelDOID:0112018Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:29007)
Molecular_infoCorresponding_CDSH09G03.2a
H09G03.2b
H09G03.2c
Corresponding_transcriptH09G03.2a.1
H09G03.2b.1
H09G03.2c.1
Other_sequence (28)
Associated_featureWBsf716537
WBsf991702
WBsf991703
WBsf991704
WBsf1014526
WBsf1014527
WBsf226326
WBsf226327
Experimental_infoRNAi_resultWBRNAi00060452Inferred_automaticallyRNAi_primary
WBRNAi00112669Inferred_automaticallyRNAi_primary
WBRNAi00006540Inferred_automaticallyRNAi_primary
WBRNAi00060451Inferred_automaticallyRNAi_primary
WBRNAi00060449Inferred_automaticallyRNAi_primary
WBRNAi00016222Inferred_automaticallyRNAi_primary
WBRNAi00049344Inferred_automaticallyRNAi_primary
WBRNAi00114833Inferred_automaticallyRNAi_primary
WBRNAi00060450Inferred_automaticallyRNAi_primary
Expr_patternExpr6274
Expr11989
Expr1013464
Expr1030895
Expr1153078
Expr2011890
Expr2030127
Drives_constructWBCnstr00003127
Microarray_results (31)
Expression_cluster (138)
Interaction (11)
Map_infoMapIIIPosition-7.34667Error0.023656
PositivePositive_cloneH09G03Inferred_automaticallyFrom CDS info
From sequence, transcript, pseudogene data
Pseudo_map_position
ReferenceWBPaper00024261
WBPaper00027555
WBPaper00032233
WBPaper00038491
WBPaper00055090
Remarkdata submitted by [Gobel V]
Map position created from combination of previous interpolated map position (based on known location of sequence) and allele information. Therefore this is not a genetic map position based on recombination frequencies or genetic experiments. This was done on advice of the CGC.CGC_data_submission
MethodGene